Cas 79834-63-2,6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione

79834-63-2

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Basic information

Product Name: 6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione
Synonyms: 6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione
CAS NO:79834-63-2
Molecular Formula:
Molecular Weight: 289.266
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione(79834-63-2)
EPA Substance Registry System: 6-(4-Fluoro-phenyl)-7-hydroxy-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione(79834-63-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 79834-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79834-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79834-63:
(7*7)+(6*9)+(5*8)+(4*3)+(3*4)+(2*6)+(1*3)=182
182 % 10 = 2
So 79834-63-2 is a valid CAS Registry Number.

79834-63-2Upstream product

79834-63-2Downstream Products

79834-68-7 6-(4-Fluoro-phenyl)-7-methoxy-1,3,5-trimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione

79834-63-2Relevant academic research and scientific papers

NEW SYNTHESIS OF 1,3-DIMETHYL-7-HYDROXYPYRROLOPYRIMIDINE-2,4(1H,3H)-DIONES (9-HYDROXY-9-DEAZATHEOPHYLLINES)

Yoneda, Fumio,Motokura, Miyuki,Otagiri, Masaki

, p. 1273 - 1276 (2007/10/02)

Treatment of 5-nitro-1,3,6-trinitrouracil with aryl aldehydes in the presence of piperidine causes the condensation to the 5-nitro-6-styryl-uracil derivatives, followed by the intramolecular cyclization including piperidine-catalyzed oxidation-reduction t

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